4.7 Review

No common denominator: a review of outcome measures in IVF RCTs

Journal

HUMAN REPRODUCTION
Volume 31, Issue 12, Pages 2714-2722

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/humrep/dew227

Keywords

IVF; outcome measures; assisted reproduction; core outcomes; live birth; IMPRINT; CROWN; infertility trial; ongoing pregnancy; reporting guidelines

Funding

  1. Doctoral Research Fellowship from the National Institute for Health Research
  2. BBSRC [BB/J021636/1] Funding Source: UKRI
  3. MRC [MR/L020335/1, G0801057, G0700092, G0300484] Funding Source: UKRI
  4. Biotechnology and Biological Sciences Research Council [BB/J021636/1] Funding Source: researchfish
  5. Medical Research Council [G0700092, G0300484, G0801057, MR/L020335/1, 1543095] Funding Source: researchfish
  6. National Institute for Health Research [DRF-2014-07-050, ICA-CDRF-2015-01-068] Funding Source: researchfish
  7. Wellbeing of Women [RG1442] Funding Source: researchfish
  8. National Institutes of Health Research (NIHR) [ICA-CDRF-2015-01-068, DRF-2014-07-050] Funding Source: National Institutes of Health Research (NIHR)

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STUDY QUESTION: Which outcome measures are reported in RCTs for IVF? SUMMARY ANSWER: Many combinations of numerator and denominator are in use, and are often employed in a manner that compromises the validity of the study. WHAT IS KNOWN ALREADY: The choice of numerator and denominator governs the meaning, relevance and statistical integrity of a study's results. RCTs only provide reliable evidence when outcomes are assessed in the cohort of randomised participants, rather than in the subgroup of patients who completed treatment. STUDY DESIGN, SIZE, DURATION: Review of outcome measures reported in 142 IVF RCTs published in 2013 or 2014. PARTICIPANTS/MATERIALS, SETTING, METHODS: Trials were identified by searching the Cochrane Gynaecology and Fertility Specialised Register. English-language publications of RCTs reporting clinical or preclinical outcomes in peer-reviewed journals in the period 1 January 2013 to 31 December 2014 were eligible. Reported numerators and denominators were extracted. Where they were reported, we checked to see if live birth rates were calculated correctly using the entire randomised cohort or a later denominator. MAIN RESULTS AND THE ROLE OF CHANCE: Over 800 combinations of numerator and denominator were identified (613 in no more than one study). No single outcome measure appeared in the majority of trials. Only 22 (43%) studies reporting live birth presented a calculation including all randomised participants or only excluding protocol violators. A variety of definitions were used for key clinical numerators: for example, a consensus regarding what should constitute an ongoing pregnancy does not appear to exist at present. LIMITATIONS, REASONS FOR CAUTION: Several of the included articles may have been secondary publications. Our categorisation scheme was essentially arbitrary, so the frequencies we present should be interpreted with this in mind. The analysis of live birth denominators was post hoc. WIDER IMPLICATIONS OF THE FINDINGS: There is massive diversity in numerator and denominator selection in IVF trials due to its multistage nature, and this causes methodological frailty in the evidence base. The twin spectres of outcome reporting bias and analysis of non-randomised comparisons do not appear to be widely recognised. Initiatives to standardise outcome reporting, such as requiring all effectiveness studies to report live birth or cumulative live birth, are welcome. However, there is a need to recognise that early outcomes of treatment, such as stimulation response or embryo quality, may be appropriate choices of primary outcome for early phase studies.

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